Canonical Allele Identifier: CA2012557415

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109189_3109190delinsGC , CM000674.2:g.3109189_3109190delinsGC	GRCh38
NC_000012.11:g.3218355_3218356delinsGC , CM000674.1:g.3218355_3218356delinsGC	GRCh37
NC_000012.10:g.3088616_3088617delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25470_-18+25471delinsGC MANE Select	ENSP00000011898.5:n.-18+25470_-18+25471delinsGC
ENST00000649909.1:c.-130+25470_-130+25471delinsGC	ENSP00000497370.1:n.-130+25470_-130+25471delinsGC
ENST00000011898.9:c.-18+25470_-18+25471delinsGC	ENSP00000011898.5:n.-18+25470_-18+25471delinsGC
ENST00000444315.6:c.-18+25470_-18+25471delinsGC	ENSP00000412908.2:n.-18+25470_-18+25471delinsGC
ENST00000537971.5:c.-18+31736_-18+31737delinsGC	ENSP00000444799.1:n.-18+31736_-18+31737delinsGC
NM_001168320.1:c.-18+31736_-18+31737delinsGC	NP_001161792.1:n.-18+31736_-18+31737delinsGC
NM_006675.4:c.-18+25470_-18+25471delinsGC	NP_006666.1:n.-18+25470_-18+25471delinsGC
XM_011520912.1:c.-349+25470_-349+25471delinsGC	XP_011519214.1:n.-349+25470_-349+25471delinsGC
XM_011520912.3:c.-349+25470_-349+25471delinsGC	XP_011519214.1:n.-349+25470_-349+25471delinsGC
NM_006675.5:c.-18+25470_-18+25471delinsGC MANE Select	NP_006666.1:n.-18+25470_-18+25471delinsGC
NM_001168320.2:c.-18+31736_-18+31737delinsGC	NP_001161792.1:n.-18+31736_-18+31737delinsGC